FDA Inspection 1063729 — Carestream Health, Inc.

Carestream Health, Inc. — FEI 1317267

The FDA completed an inspection of Carestream Health, Inc. on August 15, 2018 in Rochester, NY. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 3 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
August 15, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Rochester, NY (United States)

Citations

IDCFRDescription
328221 CFR 820.90(a)Nonconforming product, Lack of or inadequate procedures
368021 CFR 820.70(a)Process control procedures, Lack of or inadequate procedures
369621 CFR 820.100(b)Documentation